Mixed adenoneuroendocrine carcinoma of the stomach – a case report

Q4 Medicine
Marek Drab, Eva Tomsová, Juraj Marček, Tomáš Klinger
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引用次数: 0

Abstract

Neuroendocrine tumours represent a heterogeneous group of neoplasia arising from different anatomical locations, with approximately 50% of gastrointestinal origin. Main parameters in the evaluation of each case include tumour morphology, mitotic cell count, and Ki-67 index. Mixed adeno-neuroendocrine carcinomas (MANECs) are rare aggressive neoplasms consisting of both adenocarcinomatous and neuroendocrine cells, each component constituting at least 30% of the lesion. Our case represents 77-year-old polymorbid patient who, due to signs of acute bleeding in the upper gastrointestinal tract with anaemic syndrome, underwent a gastroscopic examination for melena with the finding of an ulcer lesion on the front wall of the stomach at the junction of the body and the antrum. The control gastroscopic examinations with biopsies, at first only signs of chronic gastritis with Helicobacter pylori positivity were histologically proven, then fragments of high-grade tubular to tubulovillous adenoma and structures of moderately differentiated tubular adenocarcinoma were found. Histological analysis of the gastric resection showed mixed adeno-neuroendocrine carcinoma with lymphangioinvasion.
胃混合性腺神经内分泌癌1例
神经内分泌肿瘤是一种异质性的肿瘤,起源于不同的解剖位置,大约50%起源于胃肠道。评价各病例的主要参数包括肿瘤形态、有丝分裂细胞计数、Ki-67指数。混合性腺-神经内分泌癌(MANECs)是一种罕见的侵袭性肿瘤,由腺癌细胞和神经内分泌细胞组成,每种细胞至少占病变的30%。我们的病例是一位77岁的多病患者,由于上消化道急性出血并贫血综合征的迹象,在胃镜检查中发现在身体和胃窦交界处的胃前壁有溃疡病变。对照胃镜检查和活检,起初只有幽门螺杆菌阳性的慢性胃炎的组织学证实,然后发现高级别管状到管状绒毛腺瘤的碎片和中分化管状腺癌的结构。胃切除术的组织学分析显示混合性腺-神经内分泌癌伴淋巴管浸润。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Gastroenterologie a Hepatologie
Gastroenterologie a Hepatologie Medicine-Gastroenterology
CiteScore
0.40
自引率
0.00%
发文量
32
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